A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128271



Internal ID19277337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115952105..115952486hg38UCSC Ensembl
Outerchr10:117711616..117711997hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv519n106
Supporting Variantsnssv3958546
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128271
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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